Compositions for increasing hydrocarbon production from subterranean formations

ABSTRACT

The present invention relates to a chemical composition represented by the formula: ##STR1## and ##STR2## wherein a is a whole number or fraction thereof in the range of from about 4 to about 18; 
     wherein b is a whole number or fraction thereof in the range of from about 0 to about 30; 
     wherein c is a whole number or fraction thereof in the range of from about 1 to about 3; 
     wherein d is independently a whole number or fraction thereof in the range of from about 0 to about 1 and the sum of the average values of d are less than or equal to c; 
     R is independently selected from the group consisting of hydrogen and a methyl group whereby mixtures containing both groups may result; and 
     X +  is an exchangeable cation; and 
     Z is a nucleophile containing species containing at least one member selected from the group consisting of oxygen and nitrogen wherein the nitrogen is in the form of NR 1  wherein R 1  is independently selected from the group consisting of hydrogen and methyl radicals.

Various procedures have been developed and utilized heretofore toincrease the flow of hydrocarbons from hydrocarbon-containingsubterranean formations penetrated by well bores. For example, acommonly used production stimulation technique involves creating andextending fractures in the subterranean formation to provide flowchannels therein through which hydrocarbons flow from the formation tothe well bore. The fractures are created by introducing a fracturingfluid into the formation at a flow rate which exerts a sufficientpressure on the formation to create and extend fractures therein. Solidfracture proppant materials, such as sand, are commonly suspended in thefracturing fluid so that upon introducing the fracturing fluid into theformation and creating and extending fractures therein, the proppantmaterial is carried into the fractures and deposited therein whereby thefractures are prevented from closing due to subterranean forces when theintroduction of the fracturing fluid has ceased.

In such formation fracturing and other production stimulationprocedures, it is important to leave the formation with maximumpermeability or conductivity whereby hydrocarbons contained in theformation flow to the well bore with the least possible restriction. Inorder to achieve maximum conductivity of hydrocarbons from subterraneanformations, whether or not such formations have been fractured orotherwise stimulated, it has heretofore been the practice to cause theformation surfaces to be water wet. Such water wetting has been shown toprovide an improved flow of hydrocarbons through flow channels andcapillaries in the magnitude of about three times greater than when theformation surfaces are hydrocarbon wet.

The water wetting of solid surfaces in subterraneanhydrocarbon-containing formations as well as the surfaces of solidproppant material deposited therein has heretofore been accomplishedusing surfactants whereby a layer of water or water and surfactant isspread over the solid surfaces. Such layers of water or water andsurfactant are extremely viscous near the interface of the layer and thesolid surface, and while the layer provides a slippage or lubricatingeffect at the interface thereof with hydrocarbons which decreases theresistance to flow, the layer reduces the effective diameter ofcapillaries and flow channels. This reduction of effective diameterrestricts fluid flow, and in very small capillaries or flow channelsbecomes significant, that is, when the capillary radius is equal to theviscous wetting layer thickness, the flow of hydrocarbons is blocked bythe layer.

SUMMARY OF THE INVENTION

By the present invention, methods are provided whereby certain compoundsare caused to be adsorbed onto solid surfaces and particularly surfacesof carbonate materials in subterranean hydrocarbon-containing formationsin a very thin layer, that is, a layer which is preferably one moleculethick and significantly thinner than a layer of water or awater-surfactant mixture. The compounds so adsorbed on the surfacesresist or substantially reduce the wetting of the surfaces by water andhydrocarbons and provide high interfacial tensions between the surfacesand water and hydrocarbons. This allows the hydrocarbons to displaceinjected water leaving a lower water saturation and an increased flow ofhydrocarbons through capillaries or flow channels in the formations.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a plot of the effectiveness of a perfluorosubstituted potassium phenol sulfonate of the present invention incomparison to a conventional treatment fluid.

FIG. 2 is a diagrammatic illustration of the test apparatus employed inevaluating the performance of various compositions in increasinghydrocarbon production.

DESCRIPTION OF THE PREFERRED EMBODIMENT

The compounds which are utilized in accordance with the methods of thisinvention to reduce the tendency of solid surfaces from becoming wateror hydrocarbon wet while not creating significantly thick and/or viscouslayers thereon are certain anionic perfluoro compounds and mixtures ofsuch compounds represented by the formula: ##STR3## wherein a is a wholenumber or fraction thereof in the range of from about 4 to about 18;

wherein b is a whole number fraction thereof in the range of from about0 to about 30;

wherein c is a whole number or fraction thereof in the range of fromabout 1 to about 3;

wherein d is independently a whole number or fraction thereof in therange of from about 0 to about 3 and the sum of average values of d areless than or equal to c;

R is independently selected from the group consisting of hydrogen and amethyl group whereby mixtures containing both groups may result;

X⁺ is substantially any exchangeable cation such as those selected fromthe group consisting of sodium, potassium and ammonium ions or the likeor any other cation which does not adversely react to the detriment ofthe method of the present invention; and

Z, when present, is a nucleophile containing species containing eitheroxygen in combination with the sulfonate radical, such as, for example,phenol sulfonic acid or isethionic acid or nitrogen in the form of NR¹wherein R¹ is selected from either hydrogen or methyl radicals, such as,for example, N methyl-taurine sulfonate.

The phrase "whole number or fraction thereof" as used herein indicatesthat the formula may represent an admixture of compounds wherein theaverage values of a, b, c and d can be any number in the range set forthsuch as 2 or 8 or 10 or a fraction such as 2.1, 8.5, 8.8 or 10.2 and thelike.

Preferably, in the above formulas,

a is in the range of from about 6 to about 12;

b is in the range of from about 0 to about 20;

c is in the range of from about 1 to about 2;

R is independently selected from hydrogen and methyl radicals; and

X⁺ is a cation selected from the group consisting of sodium, potassiumand ammonium ions or the like.

The preferred perfluoronated compound for use in accordance with thepresent invention is that represented by the following formula: ##STR4##

In this preferred perfluoronated compound,

a is a whole number or fraction thereof in the range of from about 6 toabout 12;

b is a whole number or fraction thereof in the range of from about 10 toabout 20;

c is a whole number or fraction thereof in the range of from about 1 toabout 2;

R is independently selected from hydrogen and methyl radicals and,preferably, is a methyl radical; and

X⁺ is a cation selected from sodium, potassium and ammonium ions.

Of this group of compounds, the most preferred is where

a is a whole number or fraction thereof in the range of from about 7 toabout 9 and, most preferably, about 8;

b is a whole number or fraction thereof in the range of from about 15 toabout 20;

c is about 1.5;

R is independently selected from hydrogen and methyl radicals and, mostpreferably, methyl; and

X⁺ is a cation selected from sodium, potassium and ammonium ions and,most preferably, potassium and ammonium ions.

In carrying out the methods of the present invention, the anionicperfluoro compound or compounds can be applied directly to asubterranean formation whereby the surfaces thereof are contacted by thecompounds and adsorbed thereon. Preferably, the anionic perfluorocompound or compounds utilized are dissolved or dispersed in a carrierfluid which is in turn introduced into the formation whereby the carriedanionic perfluoro compounds are distributed in the formation and contactsolid surfaces therein whereby they are adsorbed thereon. Aqueous orhydrocarbon base carrier fluids can be utilized in the form of liquids,foams, emulsions and so forth. The aqueous fluid can comprise, forexample, acidic solutions containing acids such as, for example,hydrochloric acid, acetic acid, formic acid and mixtures thereof or saltsolutions such as KCl, NH₄ Cl or NaCl or fresh water. The carrier fluidalso can contain other conventional additives which are compatible withthe anionic perfluoro compound of the present invention such as, forexample, nonemulsifying agents or surface tension reducing agents,mutual solvents, corrosion inhibitors, gelling agents, paraffin and ironcontrol agents and the like. The particular quantity of perfluorocompounds combined with the carrier fluid can vary widely depending uponthe type of formation to be treated and other factors, but generally theanionic perfluoro compounds utilized are combined with the carrier fluidin an amount in the range of from about 0.01% to about 0.2% by weight ofthe carrier fluid. It is to be understood that larger quantities can beemployed but such use is economically undesirable.

In carrying out subterranean formation fracturing processes wherein afracturing fluid is introduced into a subterranean formation at a ratesuch that fractures are created in the formation and extended therein,the anionic perfluoro compound or compounds utilized are convenientlycombined with the fracturing fluid prior to introducing it into theformation.

In the usual case, a non-viscous preflush solution is injected into theformation, followed by a viscous fracturing fluid without proppantmaterial which is in turn followed by a viscous fracturing fluidcarrying solid proppant material, such as sand, bauxite, glass beads orthe like. The fracturing fluids create and extend fractures in theformation and the solid proppant material is carried into and depositedin the fractures. In carrying out such fracturing procedures inaccordance with this invention, the anionic perfluoro compound orcompounds utilized can be dissolved or dispersed in the non-viscouspreflush solution as well as the viscous fracturing fluids in aconvenient manner. Upon introducing the preflush and fracturing fluidsinto the subterranean formation, the anionic perfluoro compounds areadsorbed on the solid surfaces of the formation. Thus, thecarbonate-containing surfaces of the formation have anionic perfluorocompounds adsorbed thereon whereby such surfaces are substantiallyprevented from being wetted by water or hydrocarbons and the flow ofhydrocarbons through the formation is significantly increased.

In subterranean formation fracturing procedures, cationic perfluorocompounds discussed in U.S. Pat. No. 4,425,242 can be combined with theproppant-laden fluids introduced into the formation in a sufficientquantity whereby the compounds are adsorbed on the proppant materialemployed if such proppant material has not been pretreated. Thisquantity can vary depending upon the type of formation and the quantityof proppant material utilized, but generally is in the range of fromabout 0.01% to about 0.2% by weight of the fracturing fluid and proppantmaterial used.

The Starting Perfluoro Alcohol Compounds

The starting perfluoro compounds which are used to generateperfluorinated substituents within the compositions of this inventionare derived from perfluoro substituted ethanols which are represented bythe following formula:

    F(CF.sub.2).sub.a CH.sub.2 CH.sub.2 OH                     Formula IV

In the above Formula IV, a has the numerical values previously indicatedin Formulas I and II. A preferred perfluoro ethanol is commerciallyobtained from E.I. duPont de Nemours & Co. under the commercial name"Zonyl BA". This material is generally described by Formula IV wherein ais from about 6 to about 12 and wherein the average a is equal to about8. An average a, again, indicates that the compounds used may be anadmixture of molecules wherein a is individually 6, 8, 10 or 12 and thelike with the numerical average being about 8.

The Oxiranes and Substituted Oxiranes

The starting oxirane and substituted oxirane used to initially reactwith the perfluorinated alcohols previously described are chosen fromthe group consisting of ethylene oxide, propylene oxide, butylene oxideand mixtures thereof. The preferred oxirane reactants are chosen fromthe group consisting of ethylene oxide, propylene oxide and mixturesthereof added sequentially or via mixer addition. The most preferredoxirane reactant is propylene oxide.

The Epihalohydrins

The starting epihalohydrins used to react with the perfluoronatedalcohol adducts with the oxirane compounds previously described arechosen from the group consisting of epichlorohydrin, epibromohydrin andepiiodohydrin. The preferred epihalohydrin is epichlorohydrin.

The Sulfonates

The starting compounds used to form the compounds of the presentinvention can comprise, for example, sodium, potassium or ammoniumsulfite which when reacted with the epihalohydrin forms a sulfonate, orthe previously formed sulfonates of isethionic acid or N-methyl taurine.Likewise, the starting compound can be a phenol or aniline which hasbeen sulfonated previously such as, for example, phenol sulfonic acidand the like.

The Catalysts

The catalysts used in the reactions of the perfluoro alcohol previouslydescribed, the oxirane and substituted oxirane compounds previouslydescribed, and the epihalohydrins described above are chosen from Lewisacid compounds. These catalysts are represented by antimonypentachloride, boron trichloride, boron trifluoride, stannic chloride,ferric and ferrous chloride and the like. The Lewis acid preferred inboth the reaction between the perfluoro alcohol and the oxiranecompounds, as well as between the alkoxylate adduct formed by this firstreaction and the epihalohydrin is antimony pentachloride. The catalystis used at a concentration ranging from 0.01% based on the final adductup to about 1.0% by weight based on the final adduct weight. A preferredrange of catalyst is between 0.1% and 0.5% by weight based on the finaladduct. A most preferred catalyst concentration, particularly inreference to the use of antimony pentachloride is between 0.2 and 0.4%by weight of the final adduct obtained from this combined reaction.

Reaction Conditions, Synthesis of Perfluoro Alcohol/Oxirane Compounds

The initial alkoxylate adducts required to manufacture the compounds ofthis invention are synthesized by reacting the perfluoro alcoholdescribed above with the oxirane and substituted oxirane compoundsdescribed above. This first reaction is done under anhydrous conditionsand is catalyzed by a Lewis acid catalyst, again described above. Afterthis initial alkoxylate adduct is formed, it is then reacted with anepihalohydrin to obtain the final adduct.

The reaction of the perfluoro alcohol with the oxirane and substitutedoxiranes is accomplished by using the following method or variationsthereof.

To an autoclave which has previously been charged with the perfluoroalcohol and a Lewis acid catalyst, an amount of an oxirane orsubstituted oxirane or a mixture thereof is added at such a rate so asto maintain a reaction temperature between 60° and 140° C. The reactionis catalyzed by a Lewis acid, preferably antimony pentachloride, andadditional catalyst may be added simultaneously with the addition of theoxirane/substituted oxirane compounds. The oxirane/substituted oxiranecompounds may be added in such quantities such that the molar ratio ofperfluoro alcohol to oxirane/substituted oxirane compounds is between1:4 and 1:10, and a most preferred molar ratio is between 1:6 and 1:8.The reaction rate may be controlled by using a combination oftemperature and catalyst concentration variations.

Once the oxirane/substituted oxirane compounds are completely charged tothe autoclave, the autoclave is maintained at a temperature of at least80° C. until the reaction is completed. It is preferred that theautoclave be maintained at temperatures of at least 100° C. for a timeperiod of at least 30 minutes following the completed addition of theoxirane/substituted oxirane chosen. The autoclave may be cooled and asample may be removed for analysis or for further chemical reaction.Additional oxirane/substituted oxirane also may be charged to theautoclave to obtain higher molecular ratios of perfluoro alcohol andoxirane/substituted oxirane or to vary the type of oxirane/substitutedoxirane substitution in the final product. The reaction may beconveniently monitored by analyzing unreacted oxiranes using GasChromatographic techniques. The most preferred adduct is obtained whenresidual oxirane levels are about 0.2 weight percent or below.

Alternatively, the autoclave may be maintained at reaction temperaturewhile additional catalyst and the epihalohydrin chosen to obtain thefinal adduct is added to the autoclave contents. The preferred finaladduct is again obtained when residual epihalohydrin levels are about0.2 weight percent or below as is conveniently monitored by using GasChromatographic techniques. All of the above reactions are anhydrous innature and are accomplished in an inert atmosphere such as is obtainedby a nitrogen environment.

Reaction Conditions; Synthesis of Perfluoro Alcohol/Oxirane-SubstitutedOxirane/Epihalohydrin Adduct

Once the initial alkoxylated adduct is formed using reaction conditionsdescribed above, or variations thereof, the autoclave may be cooled andthe initial alkoxylated adduct removed for further reactions. As above,the initial adduct may be reacted with quantities of epihalohydrin suchthat the desired molar ratios represented in Formulas I and II above maybe obtained. Again, reaction conditions are anhydrous, in an inertenvironment such as may be obtained with a nitrogen atmosphere, underLewis acid catalyst conditions previously described, and are bestobtained by the addition of the chosen epihalohydrin, such asepichlorohydrin, to an autoclave containing the previously reactedcompound derived from the reaction of perfluoro alcohol and theoxirane/substituted oxirane compounds.

The reaction temperatures are preferably maintained below 120° C. andthe Lewis acid catalyst is preferably used at a concentration of atleast 0.1% based on the weight of the expected final product. Thepreferred catalyst is, again, antimony pentachloride, although BF₃etherate also may be readily used. The antimony pentachloride givesfewer side reaction products and is most preferred as a catalyst forthis reaction.

The addition of epihalohydrin is maintained at a rate to control thereaction temperature below 120° C., preferably within a range between60° and 100° C. After epihalohydrin addition is completed, the reactantsare heated for at least an additional 30 minutes at a temperature ofabout 100° C. so as to obtain complete reaction. As required, additionalcatalyst may be added so as to enhance the reaction rate leading tofinal and complete reaction of all reactants. Additional epihalohydrinmay be added so as to increase the mole ratio of the final productobtained through this reaction. When the preferred adduct is obtained,such as, the adduct represented by Formulas I or II above, thesulfonation reaction may be commenced in the same autoclave or may becommenced by cooling the autoclave contents, isolating the contents or aportion thereof, and reacting this product with one of the appropriatesulfonating agents or sulfonate containing reactants previouslydescribed.

Reaction Conditions, The Sulfonation Reaction

The reaction between the perfluoro alcohol/oxirane-substitutedoxirane/epihalohydrin adduct and the sulfonate may be conducted usingeither one of the following methods as well as any other method whichresults in the desired reaction.

The epihalohydrin adduct of the oxirane substituted perfluoro alcohol isisolated in a reaction vessel and diluted to about a 50 percent activesolution utilizing a 50:50 mixture by weight of isopropanol and water.An equimolar amount of an aqueous solution of sodium or ammoniumbisulfite is added to the reaction vessel and the mixture is stirred atambient temperature for about one hour. This procedure produces asulfonate through dehydrohalogenation and sulfite addition.

Alternatively, the epihalohydrin adduct of the oxirane substitutedperfluoro alcohol is diluted to about a 33 percent active solutionutilizing a 50:50 mixture by weight of isopropanol and water and placedin an autoclave. An equivalent of phenol sulfonic acid, taurinesulfonate or sulfonated aniline then is admixed with the dilutedmixture. The acid then is neutralized with an equivalent of potassiumcarbonate. When the acid is phenol sulfonic acid, an additionalequivalent of potassium carbonate is added to the mixture to form aphenolate anion. The phenolate or amines present react with theepihalohydrin adduct to form the desired sulfonate derivative uponstirring the mixture in the autoclave for about two hours at atemperature of about 125° C.

EXAMPLES

I. Alkoxylates--the formation of the initial adduct between theperfluoro alcohol and the oxirane/substituted oxirane compounds.

A. Ethylene Oxide (EO)

EXAMPLE 1

To a PARR autoclave is added 485 grams (1 mole) Zonyl BA alcohol and 1cc of antimony pentachloride. The autoclave was closed and heated to 50°C. Three hundred fifty-two (352) grams (approximately 8 moles) ofethylene oxide was slowly added to the autoclave, the addition ratebeing controlled in such a manner as to maintain the reactiontemperature below 100° C. After at least 1/2 of the EO was added, theaddition rate was increased in such a manner as to allow the reactiontemperature to slowly rise to 140° C. After the addition of ethyleneoxide was completed, the autoclave temperature was maintained at130°-140° C. for one hour. The contents of the autoclave were thencooled and removed from the autoclave. The reaction product is the mixedalkoxylate expected from the addition of 8 moles of ethylene oxide to 1mole of the Zonyl BA perfluoro alcohol.

EXAMPLE 2

Four hundred eighty-five (485) grams of the Zonyl BA alcohol and 1 cc ofantimony pentachloride was added to an autoclave and heated to 50° C.Four hundred forty (440) grams (10 moles) of EO was added slowly so asto maintain reaction temperature below 100° C. Reaction temperature maybe controlled by the addition rate of EO or by adjusting the rate ofcooling of the PARR autoclave using external cooling coils. After about1/3 of the ethylene oxide was added, the reaction temperature wasallowed to rise to 140° C. After the addition of EO was completed, thereaction vessel temperature was maintained between 130°-140° C. forapproximately one hour by heating this reaction vessel. The content werecooled and removed from the autoclave. The reaction product is thatexpected from the 10 mole addition of ethylene oxide to the Zonyl BAperfluoro alcohol previously described.

EXAMPLE 3

The conditions of Examples 1 and 2 were repeated except that 15 moles ofethylene oxide were added at such a rate as to control the reactiontemperature below 140° C. The product mix obtained was that expectedfrom the 15 mole addition of ethylene oxide to the perfluoro alcohol.

B. Propylene Oxide (PO)

EXAMPLE 4

To an autoclave was added 485 grams (1 mole) of the Zonyl BA perfluoroalcohol. The autoclave was purged with nitrogen and 2 cc of antimonypentachloride was added. The autoclave was closed to the atmosphere andheated to 50° C. while stirring. Two moles (about 108 grams) of PO wasslowly added to the reaction vessel at a rate sufficient to maintain thereaction temperature below 100° C. Addition of the propylene oxiderequired approximately one hour. The autoclave contents were then heatedfor another hour at a temperature of 90° C. The reactor was cooled andapproximately 666 grams of this 2 mole adduct of the perfluoroalcohol/propylene oxide alkoxylate was removed for further reaction.

EXAMPLE 5

To the materials remaining in the autoclave from Example 4 was added 108grams of additional propylene oxide. The initial temperature at thestart of the reaction was 52° C. The vessel was depressurized andanother 0.5 mls of antimony pentachloride catalyst was added. Additionof the propylene oxide was reinitiated. The temperature of the reactionvessel was less than 80° C. throughout the addition of propylene oxide.The heat source was turned off and the autoclave allowed to coolovernight. The next day, the contents of the autoclave were determinedto be the 4 mole adduct of propylene oxide of the perfluoro alcohol.

EXAMPLE 6

Three hundred (300) grams of the alkoxylate adduct obtained from Example4 was charged to a PARR autoclave along with 5/8 cc of antimonypentachloride. The reactor was purged with nitrogen and heated to 50° C.Addition of propylene oxide was begun. Sufficient propylene oxide wasadded to the reactor to obtain a 6 mole propylene oxide adduct onto theperfluoro alcohol. The propylene oxide addition rate was maintained soas to control the reaction temperature below 100° C. during the additionof propylene oxide. The reaction vessel was heated for an additionalhour after the addition of propylene oxide was completed at atemperature of 100° C. The reaction vessel was cooled and the 6 moleadduct of the perfluoro alcohol was removed from the reactor.

EXAMPLE 7

Three hundred (300) grams of the adduct from Example 4 was charged to aPARR autoclave along with 1 milliliter of antimony pentachloride. Thesame precautions were taken as in Example 6 to maintain reactiontemperatures and to maintain a nitrogen atmosphere. Sufficient propyleneoxide was added to obtain a 10 mole propylene oxide adduct of the ZonylBA perfluoro alcohol.

C. Mixed Oxide Alkoxylate

EXAMPLE 8

To a PARR autoclave was added 485 grams (1 mole) perfluoro alcohol and 2milliliters of antimony pentachloride. The reactor was purged withnitrogen and closed to the atmosphere. The reactor contents were heatedto 50° C. while they were being stirred. Ten moles of ethylene oxidewere slowly added to the reactor contents at a rate sufficient tomaintain the temperature of the reactor below 100° C. The reactor washeated at a temperature of 100° C. for 1.5 hours after the addition ofall of the ethylene oxide. After this heating period, 5 moles ofpropylene oxide were slowly added so as to maintain the reactortemperature at 100° C. The reactor contents were then agitated for anadditional hour and the temperature was allowed to rise slowly to 130°C. The temperature was maintained at 130° C. for an hour after all theethylene oxide had been added. The autoclave was cooled andapproximately 1,220 grams of the final alkoxylate adduct were recovered,demonstrating essentially 100% recovery.

II. The Reaction Between Alkoxylates and Epihalohydrin.

EXAMPLE 9

To an autoclave was added 485 grams of Zonyl BA perfluoro alcohol and 2milliliters of antimony pentachloride catalyst. The autoclave was purgedwith nitrogen and closed to the atmosphere. The autoclave was heated to60°-70° C. for about 30 minutes. A mixture of 330 grams of ethyleneoxide and 442 grams of propylene oxide was slowly added to the stirredcontents of the autoclave. The addition rate of this mixed oxidesolution was controlled such that the temperature never exceeded 90° C.and, in fact, remained in the 75°-85° C. range. The temperature wasmaintained for about 90 minutes after the addition of the mixed oxidewas complete.

To the contents of the PARR autoclave was then added 170 grams orapproximately 1.5 moles of epichlorohydrin. hydrin. The same reactionconditions and temperature ranges were maintained as above. Anadditional 60 minutes of reaction time was allowed after the addition ofepichlorohydrin was complete so as to complete the reaction between theepichlorohydrin and the mixed alkoxylate obtained in the previousreaction step.

EXAMPLE 10

Two hundred four (204) grams of an 8 mole EO adduct of the Zonyl BAperfluoro alcohol and 0.25 milliliter of BF₃ etherate were placed in a500 milliliter flask. The flask was equipped with a condenser, astirrer, a thermometer, and a pressure equalized dropping funnel. Thismixture was heated to 50° C. and a nitrogen purge was initiated.Dropwise addition of epichlorohydrin was started. The reactiontemperature was held between 55°-60° C. by regulating the rate ofaddition of epichlorohydrin. Approximately 34.5 grams of epichlorohydrinwas added to the flask contents over a period of one hour. The reactioncontents were postheated for approximately 1.5 hours, then cooled andremoved from the flask. The product was an adduct of the perfluoroalcohol/8 mole ethylene oxide/1.5 mole epichlorohydrin. Product yield asjudged by the weight of recovered material is 98+%.

EXAMPLE 11

Into 3 separated flasks equipped as in Example 10, products from sectionI.B., Examples 4, 5 and 6, were independently charged. Sufficient BF₃etherate was added to the contents of each flask and the flasks heatedto approximately 50° C. Nitrogen purges were started on each flask.Epichlorohydrin was added to each flask so as to yield a 2 moleepichlorohydrin adduct to the materials obtained from Example 4, and a1.5 mole epichlorohydrin adduct from both the materials of Examples 5and 6. The epichlorohydrin was added at a rate which maintained thetemperature of each reaction vessel at less than 95° C. Again eachreaction vessel was postheated for approximately one hour attemperatures not exceeding 95° C. The products obtained in each casewere respectively those expected from (1) a 1:2:2 mole adduct ofperfluoro alcohol/propylene oxide/epichlorohydrin; (2) a 1:4:1.5 moleadduct of perfluoro alcohol/propylene oxide/epichlorohydrin; and (3) a1:6:1.5 mole adduct of perfluoro alcohol/propylene oxide/epichlorohydrinadduct.

EXAMPLE 12

One mole of a product obtained from following the first step of Example9 is added to a 500 ml flask equipped as above. Sufficientepibromohydrin to obtain a 1 mole adduct is slowly added to thismaterial after it is heated to approximately 50° C. and 1 milliliter ofantimony pentoxide is added to the flask. The epibromohydrin additionrate is controlled such that the reaction temperature never exceeds 100°C. The product expected is a 1:2:2:1.0 molar adduct of perfluoroalcohol/ethylene oxide/propylene oxide/ and epibromohydrin.

III. The Sulfonation Reaction.

EXAMPLE 13

To a reaction flask was added the 8 mole ethylene oxide adduct of ZonylBA perfluoro alcohol of Example 10. The adduct was dissolved in a 50:50mixture by weight of isopropanol and water in an amount sufficient toprovide about a 33 percent active solution. To the diluted mixture wasadded an equimolar amount of sodium bisulfite in the form of about a 40percent aqueous solution. The mixture then was stirred for about onehour at ambient temperature. The resulting product was found to be theisopropyl sulfonate ether of the 8 mole ethylene oxide adduct of ZonylBA perfluoro alcohol.

EXAMPLE 14

To a reaction flask was added a quantity of a 4 mole ethylene oxideadduct of Zonyl BA perfluoro alcohol prepared in accordance with theforegoing procedures. The adduct is dissolved in a 50:50 mixture byweight of isopropanol and water in an amount sufficient to provide abouta 30 percent active solution. To the diluted mixture was added anequimolar amount of N-methyl taurine. The contents of the reaction flaskthen were heated to a temperature of about 60° C. and refluxed for aboutone hour. The resulting product was found to be the isopropyl-N-methyltaurine sulfonate ether of the 4 mole ethylene oxide adduct of Zonyl BAperfluoro alcohol.

EXAMPLE 15

To a reaction flask was added the 10 mole ethylene oxide adduct of ZonylBA perfluoro alcohol prepared in Example 2. The adduct was reacted with1.5 moles of epichlorohydrin as previously described and the resultingoxirane epichlorohydrin adduct of Zonyl BA perfluoro alcohol then wasdiluted with dimethyl sulfoxide in a ratio of adduct to sulfoxide of 1to 3. To the diluted mixture in the reaction flask was added a molarequivalent of potassium phenol sulfonate. The contents of the flask thenwere heated to about 38° to 40° C. for about one hour. The resultingproduct, as expected, was found to be the isopropyl potassium phenolsulfonate ether of the 10 mole ethylene oxide adduct of Zonyl BAperfluoro alcohol.

EXAMPLE 16

To a reaction flask was added a quantity of an 8 mole propylene oxideadduct of Zonyl BA perfluoro alcohol prepared in accordance with theforegoing procedures. The adduct was dissolved in the flask in a 75:25mixture by weight of isopropanol and water in an amount sufficient toprovide about a 33 percent active solution. To the mixture in the flaskthen was added an equimolar amount of sulfanilic acid. The contents ofthe reaction flask then were heated to a temperature of about 60° C. andrefluxed for about 1 hour. The resulting product was, as expected, foundto be the isopropyl sulfanilic acid adduct of the 8 mole propylene oxideadduct of the Zonyl BA perfluoro alcohol.

EXAMPLE 17

To a Parr autoclave was added the 10 mole ethylene oxide/5 molepropylene oxide adduct of Zonyl BA perfluoro alcohol of Example 8. Theadduct was dissolved in a 50:50 mixture by weight of isopropanol andwater in an amount sufficient to provide about a 33 percent activesolution. To the diluted mixture was added one equivalent of phenolsulfonic acid and two equivalents of potassium carbonate. The mixturethen was heated to a temperature of about 125° C. for about two hours.The resulting product was found to be as expected the isopropyl phenolpotassium sulfonate ether of the 10 mole ethylene oxide/5 mole propyleneoxide adduct of Zonyl BA perfluoro alcohol.

EXAMPLE 18

To a Parr autoclave was added a quantity of a 15 mole mixed ethyleneoxide and propylene oxide adducts of Zonyl BA perfluoro alcohol. Theadducts were dissolved in a 75:25 mixture by weight of isopropanol andwater in an amount sufficient to provide about a 33 percent activesolution. To the diluted mixture was added one equivalent of phenolsulfonic acid and two equivalents of potassium carbonate. The contentsof the autoclave then were heated to a temperature of about 125° C. forabout two hours. The resulting product was found to be, as expected, theisopropyl phenol potassium sulfonate ether of the 15 mole mixed ethyleneoxide/propylene oxide adduct of Zonyl BA perfluoro alcohol.

In order to facilitate a clear understanding of the methods of thepresent invention, the following examples are provided.

EXAMPLE 19

To illustrate the effectiveness of the compositions of the presentinvention in enhancing liquid and gaseous hydrocarbons permeability in alimestone matrix and improving the return of treating fluids by loweringcapillary pressure, the following tests were performed. The testsutilize a dolomite column which is treated with fluids containing thecomposition of the present invention in an amount of from about 0.01 toabout 0.1 percent by weight. The percent treating fluid recovered athydrocarbon breakthrough is measured and the water saturation of thedolomite column, at each flowing pressure is calculated to permit thepreparation of a plot of capillary pressure versus water saturation.FIG. 1 illustrates a plot of the effectiveness of a perfluorosubstituted potassium phenol sulfonate of the present invention (FormulaII: a=8, b=0, c=1, Z=oxygen and d=1) in comparison to a conventionaltreatment utilizing 2% KCl. The treatment with 2% KCl results in about a28 percent recovery of treating fluid at oil breakthrough in the columnwhile the use of the composition of the present invention in a 0.01percent concentration provides about a 90 percent recovery of treatingfluid at oil breakthrough. Also, the presence of the composition of thepresent invention dramatically shifts the capillary pressure curve asillustrated in FIG. 1. While the 2% KCl exhibits a capillary pressure ofabout 20 psi at about 30 percent water saturation (S_(w)), the columntreated with the composition of the present invention exhibits acapillary pressure of about 2.5 psi at about 30 percent S_(w).

A final measurement of overall treatment effectiveness is the effectivepermeability of the formation to hydrocarbon flow at each equilibriumwater saturation. For example, the control sample comprising 2% KClutilized in the oil flow experiment provided a relative permeability tooil (k_(o)) of about 3.49 at a 1.0 cc/min flow rate and about 5.18 at 10cc/min. By way of contrast, the use of the composition of the presentinvention in the treatment of a carbonate-containing formation resultsin an effective permeability that significantly exceeds that of thecontrol fluid and commonly available surfactants. Further, thepercentage of treating fluid recovered at hydrocarbon breakthrough ismaximized by use of the composition of the hydrocarbon breakthrough ismaximized by use of the composition of the present invention. Forexample, the composition of the present invention previously identified(Formula II: a=8, R=hydrogen, b=0, c=1.5, Z=oxygen and d=1) provided 100percent treating fluid recovery and a k_(o) of about 7.57 at 10 cc/min.In the gas flow experiments, a composition of the present invention(Formula III: a=8, R=CH₃, b=15, c=1.5 and Z=oxygen) resulted in atreating fluid recovery of about 85 percent while a k_(g) of 4.23 wasachieved at 10 psi gas pressure.

Test Procedure:

A packed column having a 3/4" O.D. and about 12 in. length is preparedwith sieved 100-200 mesh dolomite and placed in the test systemillustrated in FIG. 2. API standard brine is flowed into the packedcolumn at a rate of 1.0 cc/min until the column is saturated. The timerequired to achieve saturation is about 10 minutes. The pore volume ofthe packed column then is determined by well known techniques.

For experimental tests utilized in the determinations of oilbreakthrough, a refined hydrocarbon oil then is flowed through thepacked column in the reverse direction to prior brine flow at a rate of1.0 cc/min to obtain a residual water saturation level within thecolumn. Thereafter, one pore volume of the treating fluid containing0.01 percent by weight of the designated composition of the presentinvention is flowed into the column in the same direction as thepreviously introduced brine at a rate of 1 cc/min. The treating fluidalso contained 2% KCl and a nonemulsifier consisting of an alkoxylatedphenol formaldehyde resin and various ethoxylated components. A quantityof the refined oil then is flowed in the opposite direction of thetreating fluid at sequential rates of about 0.5 cc/min, 1.0 cc/min, 5.0cc/min and 10.0 cc/min for two hours at each rate. The volume of brineand treating fluid recovered and the pressure is measured at each of thevarious flow rates as well as the percent of the treating fluidrecovered at oil breakthrough. The equilibrium water saturation withinthe packed column and the relative oil permeability then are calculatedat each oil flow rate by known techniques.

For experimental tests utilized in the determination of gasbreakthrough, nitrogen gas is flowed through the brine saturated packedcolumn at 10 psi pressure in the reverse direction to prior brine flowto obtain a residual water saturation level within the column. Thecolumn then is treated with the composition of the present invention aspreviously described together with an amphoteric surface tensionreducing agent and a mutual solvent. The flow of nitrogen gas throughthe packed column then is resumed in the opposite direction of thetreating fluid at sequential pressures of 1.0, 2.0, 5.0 and 10 psi fortwo hours at each rate. The fluid recovered and gas flow rate at eachpressure is determined as well as the percent of the treating fluidrecovered at gas breakthrough. The equilibrium water saturation withinthe packed column then and the effective permeability to gas arecalculated at each pressure level of the sequential gas flows.

The effectiveness of the various perfluoro-substituted anionic compoundsof the present invention in lowering capillary pressure and improvingaqueous treatment fluid recovery and hydrocarbon permeability inlimestone matrices is summarized in Table I and Table II, below.

                  TABLE I                                                         ______________________________________                                        Water Recovery and Capillary Pressure Measurements                            Employing Perfluoro-Substituted Sulfonates                                    in Oil                                                                                 Water Recovery                                                                           Capillary Pressure Data                                            at Oil     Oil                                                                Breakthrough                                                                             Flow                                                                 (% Treat-        (cc/                                              Composition                                                                              ment Fluid)                                                                             (Sw)   min)  (Δ P)                                                                        (Sw) k.sub.o                           ______________________________________                                        2% KCl     28        72     0.5   1.56 71.0 2.60                                                          1.0   2.32 63.7 3.49                                                          5.0   8.42 38.2 4.80                                                          10.0  15.62                                                                              32.0 5.18                              Formula III:                                                                             100       36     0.5   2.7  31.0 1.50                              (a=8, R=hydro-              1.0   3.2  27.0 2.53                              gen, b=0, c=1.5)            5.0   7.6  26.0 5.32                                                          10.0  10.7 26.0 7.57                              Formula III:                                                                             78        52      0.5* 21.0 50.0 0.19                              (a=8, R=hydro-              1.0   40.0 44.0 0.20                              gen, b=15,                  4.0   180.0                                                                              40.0 0.18                              c=1.5)                                                                        Formula III:                                                                             89        47      0.5* 90.0 47.0 0.04                              (a=8, R=CH.sub.3,           1.0   190.0                                                                              39.0 0.04                              b=8, c=1.5)                 2.0   310.0                                                                              36.0 0.05                              Formula III:                                                                             100       30     0.5   2.2  20.0 1.84                              (a=8, R=CH.sub.3,           1.0   3.1  25.0 2.61                              b=15, c=1.5)                5.0   5.3  24.0 7.64                                                          10.0  12.0 22.0 6.75                              Formula III:                                                                             96        41     0.5   1.63 36.0 2.48                              (a=8, mixed                 1.0   2.30 32.0 3.52                              oxide adduct                5.0   7.05 32.0 5.74                              having order                10.0  12.40                                                                              30.0 6.53                              of addition                                                                   of R=hydrogen                                                                 b=10 and                                                                      R=CH.sub.3, b=5,                                                              c=1.5)                                                                        Formula I: 85        39     1.0   1.88 34.0 4.30                              (a=8, R=hydro-              0.5   2.64 36.6 1.53                              gen, b=8, c=1.5)            1.0   3.53 29.0 2.29                                                          5.0   10.23                                                                              26.7 3.95                                                          10.0  19.13                                                                              26.0 4.23                              Formula I: 88        39     1.0   1.88 34.0 4.30                              (a=8, R=hydro-              0.5   2.64 36.6 1.53                              gen, b=10,                  1.0   3.53 29.0 2.29                              c=1.5)                      5.0   10.23                                                                              26.7 3.95                                                          10.0  19.13                                                                              26.0 4.23                              ______________________________________                                         *Emulsion formed resulting in plugging of column due to incompatibility       with selected nonemulsifying agent                                       

                  TABLE II                                                        ______________________________________                                        Water Recovery and Capillary Pressure Measurements                            Employing Perfluoro-Substituted Sulfonates                                    in Gas                                                                                       % Water                                                                       Recovery Capillary                                                            at Gas   Pressure Data                                                   Concen-                                                                              Breakthrough                                                                             P                                                 Composition tration  (%)     (Sw) (psi)                                                                              (Sw) k.sub.g                           ______________________________________                                        2% KCl               45      73   1.0  89.5 0.00                                                                2.0  55.9 1.20                                                                5.0  43.5 2.90                                                                10.0 31.6 3.95                              Formula III:                                                                              .01%     70      66   1.0  67.0 0.00                              (a=8, R=hydro-                    2.0  48.0 1.33                              gen, b=0, c=1.5)                  5.0  39.0 2.43                                                                10.0 37.0 2.89                              Formula III:                                                                              .1%      69      66   1.0  67.0 0.00                              (a=8, R=hydro-                    2.0  48.0 1.33                              gen, b=0, c=1.5)                  5.0  39.0 2.43                                                                10.0 37.0 2.89                              Formula III:                                                                              .1%      78      62   1.0  76.0 0.00                              (a=8, R=hydro-                    2.0  73.0 0.00                              gen, b=8, c=1.5)                  5.0  44.0 0.23                                                                10.0 30.0 0.69                              Formula III:                                                                              .01%     54      73   1.0  77.0 0.00                              (a=8, R=hydro-                    2.0  47.0 1.56                              gen, b=15, c=1.5)                 5.0  35.0 4.27                                                                10.0 33.0 4.32                              Formula III:                                                                              .1%      100     37   1.0  52.0 0.00                              (a=8, R=hydro-                    2.0  50.0 0.00                              gen, b=15, c=1.5)                 5.0  37.0 0.00                                                                10.0 29.0 0.11                              Formula III:                                                                              .01%     52      75   1.0  75.0 0.00                              (a=8, R=CH.sub.3,                 2.0  51.0 1.61                              b=8, c=1.5)                       5.0  40.0 2.94                                                                10.0 38.0 3.58                              Formula III:                                                                              .1%      76      63   1.0  65.0 0.00                              (a=8, R=CH.sub.3,                 2.0  51.0 1.33                              b=8, c=1.5)                       5.0  44.0 4.00                                                                10.0 38.0 4.46                              Formula III:                                                                              .01%     85      58   1.0  60.0 0.00                              (a=8, R=CH.sub.3,                 2.0  42.0 2.02                              b=15, c=1.5)                      5.0  36.0 3.08                                                                10.0 30.0 4.32                              Formula III:                                                                              .1%      85      60   1.0  65.0 0.00                              (a=8, R=CH.sub.3,                 2.0  50.0 2.76                              b=15, c=1.5)                      5.0  47.0 4.18                                                                10.0 43.0 4.23                              Formula III:                                                                  (a=8, R=CH.sub.3,                                                             b=15, c=1.5)                                                                  Formula III:                                                                              .1%      100     44   1.0  49.0 0.00                              (a=8, mixed                       2.0  47.0 0.00                              oxide adduct                      5.0  45.0 0.00                              having order                      10.0 25.0 1.15                              of addition                                                                   of R=hydrogen                                                                 b=10 and R=CH.sub.3,                                                          b=5, c=1.5)                                                                   ______________________________________                                    

While particular embodiments of the invention have been described, it isto be understood that such descriptions are presented for purpose ofillustration only and that the invention is not limited thereto and thatreasonable variations and modifications, which will be apparent to thoseskilled in the art, can be made without departing from the spirit orscope of the invention as defined by the following claims.

What is claimed is:
 1. A composition of matter comprising an anionicperflurosubstituted compound having a representative formula selectedfrom the group consisting of: ##STR5## and ##STR6## wherein a is a wholenumber or fraction thereof in the range of from about 4 to about18;wherein b is a whole number or fraction thereof in the range of fromabout 0 to about 30; wherein c is a whole number or fraction thereof inthe range of from about 1 to about 3; wherein d is independently a wholenumber or fraction thereof in the range of from about 0 to about 1 andthe sum of the average values of d are less than or equal to c; R isindependently selected from the group consisting of hydrogen and amethyl group whereby mixtures containing both groups may result; and X⁺is an exchangeable cation; and Z is a nucleophile containing radicalspecies containing at least one member selected from the groupconsisting of oxygen and nitrogen wherein the nitrogen is in the form ofNR¹ wherein R¹ is independently selected from the group consisting ofhydrogen and methyl radicals.
 2. The composition of claim 1 wherein:a isfrom about 6 to 12; b is from about 0 to 20; c is from about 1 to 2; andthe sum of the average values of d is from about 0 to
 2. 3. Thecomposition of claim 1 wherein:a is from about 6 to 12; b is from about10 to 20; c is about 1.5; the sum of the average values of d is about1.5; and X is selected from potassium and ammonium ions.
 4. Thecomposition of claim 3 wherein:a is from about 7 to 9 and b is fromabout 15 to
 20. 5. The composition of claim 4 wherein a is about
 8. 6. Acomposition of matter represented by the formula: ##STR7## wherein a isa whole number or fraction thereof in the range of from about 6 to about12;wherein b is a whole number or fraction thereof in the range of fromabout 10 to about 20; wherein c is a whole number or fraction thereof inthe range of from about 1 to about 2; R is independently selected fromhydrogen and a methyl radical; and X⁺ is a cation selected from thegroup consisting of sodium, potassium and ammonium ions.
 7. Thecompostion of claim 6 wherein:a is from about 7 to about 9; b is fromabout 15 to about 20; and c is about 1.5.
 8. The composition of claim 6wherein a is about
 8. 9. The composition of claim 8 wherein X isselected from the group consisting of potassium and ammonium ions.
 10. Acomposition of matter represented by the formula: ##STR8## wherein: a isa whole number or fraction thereof in the range of from about 6 to about12;b is a whole number or fraction thereof in the range of from about 10to about 20; R is independently selected from hydrogen and a methylradical; and X⁺ is a cation selected from the group consisting ofsodium, potassium and ammonium ions.
 11. The composition of claim 10wherein:a is from about 7 to about 9; b is from about 15 to about 20; Ris hydrogen; and X is selected from the group consisting of potassiumand ammonium ions.
 12. The composition of claim 11 wherein a is about 8,d is about 1.5 and e is about 1.5.
 13. The composition of claim 10wherein:a is about 8; b is about 15 to 20; R is hydrogen; and X isselected from the group consisting of potassium and ammonium ions.
 14. Asulfonic acid or salt product produced by the process comprising thesteps of:contacting a perfluoro alcohol of the formula

    F(CF.sub.2).sub.a CH.sub.2 CH.sub.2 OH

wherein a is a whole number or fraction thereof of from 4 to 18 with anoxirane selected from the group consisting of ethylene oxide, propyleneoxide, butylene oxide, mixtures thereof, and substituted derivativesthereof in the presence of a sufficient quantity of a Lewis acidcatalyst in a reaction vessel in a manner so as to maintain a reactiontemperature between 60° C. and 140° C. whereby a reaction productcomprising a perfluoro alcohol-oxirane adduct containing from about 0 toabout 30 moles of said oxirane is produced; contacting said reactionproduct in a reaction vessel with an epihalohydrin in the presence of asufficient quantity of a Lewis acid catalyst at a temperature within therange of from about 60° C. to about 100° C. whereby from 1 to 3 moles ofsaid epihalohydrin are incorporated into said reaction product; andcontacting said epihalohydrin-containing reaction product with asulfonating agent in a reaction vessel under suitable conditions wherebysaid reaction mixture is caused to yield a sulfonic acid or salt of saidepihalohydrin-containing reaction product.